Eha Lotion
NDC Package 76420-351-30

View Billable Units, 11-Digit Conversion Format, and RxNorm mappings
Table of Contents
    1. Package Information
    2. Frequently Asked Questions

Package Information

Eha (lidocaine hydrochloride) lotions is for adults and children two-years or older, apply externally to the affected area. This formulation utilizes a lotion delivery system. Marketed by Asclemed Usa, Inc., this product is identified by NDC 76420-351.

Identification & Billing

NDC Package Code
76420-351-30
Package Description
88 mL in 1 BOTTLE
Product Code
76420-351
11-Digit Billing Format
76420035130
Billing Unit
ML - Billing unit of "milliliter" is used when a product is measured by its liquid volume.
Units Per Package
88 ML

Clinical Specifications

Proprietary Name
Eha
Non-Proprietary Name
Lidocaine Hydrochloride
Substance Name
Lidocaine Hydrochloride
Dosage Form
Lotion - An emulsion, liquid1 dosage form. This dosage form is generally for external application to the skin.2
Administration Route
Topical - Administration to a particular spot on the outer surface of the body. The E2B term TRANSMAMMARY is a subset of the term TOPICAL.
Active Ingredient(s)
LIDOCAINE HYDROCHLORIDE 4 g/mL
Pharmacologic Class
Usage Information
For adults and children two-years or older, apply externally to the affected area. Do not use more than three to four times per day.

Regulatory & Marketing

Labeler Name
Asclemed Usa, Inc.
Product Type
Human Prescription Drug
Marketing Category
UNAPPROVED DRUG OTHER - An unapproved drug product in a marketing category that is not reflected on a particular list.
Start Marketing Date
06-07-2016
Listing Expiration
12-31-2026
Exclude Flag
N
Sample Package
No

Hierarchy Structure

Code Lineage

The NDC Directory contains ONLY information on final marketed drugs submitted to FDA electronically by labelers. A labeler might be a manufacturer, re-packager or re-labeler. The product information included in the NDC directory does not indicate that FDA has verified the information provided by the product labeler. Assigned NDC numbers are not in any way an indication of FDA approval of the product.

* Please review the full disclaimer at the bottom of this page.

Frequently Asked Questions

What is the distribution configuration for this product package?

The code 76420-351-30 identifies a specific commercial package of 88 ml in 1 bottle of Eha, a human prescription drug labeled by Asclemed Usa, Inc.. This product is billed per "ML" milliliter and contains an estimated amount of 88 billable units per package. This lotion is formulated for topical use and contains lidocaine hydrochloride as the active substance.

Is this product currently listed with the FDA?

Yes, this product is active and verified within the NDC Directory. It was introduced to the market by Asclemed Usa, Inc. on June 07, 2016. The current certification is valid through December 31, 2026.

How is this Asclemed Usa, Inc. product billed for insurance claims?

For medical billing and reimbursement, this package follows the 11-digit CMS format: 76420035130. Quantities are measured in per "ml or milliliter", products billed per milliliter are usually products measured by liquid volume.. There are 88 total billable units per package. The table below illustrates the segment conversion from the 10-digit labeler code to the 11-digit provider format.

11-Digit Code Conversion

Billing payers usually require a 5-4-2 segment configuration. Below is the conversion from the 10-digit package format to the 11-digit billing format:

10-Digit Format (5-3-2)
76420-351-30
11-Digit CMS (5-4-2)
76420-0351-30

Note: The zero is added to the Product segment to maintain the 5-4-2 structure.